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Introduction

As an inhibitor of the enzyme 3-hydroxy-3-methylglutaryl CoA reductase, lovastatin plays a significant role in cholesterol biosynthesis, and is therefore a medicinal compound used against cardiovascular diseases [1]. It is a naturally occurring drug which is found in foods such as oyster mushrooms and red yeast rice. In industrialized production of lovastatin, the natural producer Aspergillus terreus is used. Howere, toxins also occur during the production. Thus, a host with the potential to produce lovastatin more securely is needed. The perfect performance of Aspergillus niger in industrial production of organic acid producer makes it an inviting host for our project. Moreover, it seems to be a wise choice as there is a lot of industry experience about A. niger which has high similarity to A. terreus. In this project, the potential of A. niger to biosynthesis lovastatin are assessed by cloning and transferring the genes from A. terreus to the same species funges A. niger. Also the lovastatin resistance of A. niger is in consideration.

Rationale

For the biosynthesis of lovastatin, A. terreus uses a range of enzymes, such as polyketide synthases (PKS), enoyl reductase, esterase and a cytochrome P450 oxygenase[2]. Among these, LovB (lovastatin nonaketide synthase), LovG (thioesterase) [3]. and LovC (enoyl reductase) together take charge of most of the production pathway by releasing the intermediate-dihydromonacolin L acid from nine malonyl-CoA units [3] after 35 reactions.

LovB contains β-ketosynthase (KS), acyl transferase (MAT), dehydratase (DH), methyl transferase(MT), ketoreductase(KR), acyl carrier protein (ACP), nonribosomal-peptide synthase condensation (CON) domains and an inactive enoyl reductase (ER) domain, which is active in LovC [2][4]. The amino acid sequences of LovB and LovC were obtained of the predicted proteome of A. terreus and the functionality of some of these domains has previously been demonstrated by experiments [5].

Aim

We set out to prove that A. niger is an suitable candidate host for lovastatin production. By cloning the enzymes LovB (3038 Amino Acids (AA)), LovG (256 AA) and LovC (363 AA), which play significant roles in the lovastatin biosynthesis pathway, they can be expressed in the new genomic context. In addition, we decided to split LovB into single domains during cloning, checking the possibilty to reassemble and fuse those domains as a new biosynthetic engineering strategy.

Approach

Domain separation

The minimal polyketide synthase domains of LovB as standalone proteins have never been clearly defined nor have their activities and substrate specicifities been systematically assayed. With the help of literature, Domcut and BLAST to define the boundaries of each domain, we are able to, though theoretically, split enzymes into separate domains, while maintaining their individual functionality. By splitting enzymes into separate domains, it would be possible to rearrange domains from different sources and to design purposive multidomain enzymes producing novel products.

gBlocks and Gibson assembly

gBlocks gene fragments were ordered for cloning each domain with codon optimized sequences for A. niger. Those fragments are chemically synthesized, double-stranded DNA that are compatible with a wide range of existing applications. They are normalized to 200 ng and delivered dried down which could be obtained by adding TE buffer to the tube before briefly vortexing and centrifugation. Gibson assembly method was used to fuse the fragments together. After the gene was assembled by Gibson assembly in E. coli, it would be isolated and digested before inserting into an A. niger compatible vector for transformation and subsequent expression (Figure 1).

Figure 1: Assembly method for diversity of LovB domain complexes.

Design for modular fusion

To meet the criteria: (i). make the fusion of single or multiple domains possible (ii). a stop codon is only introduced when the domain is the last or single one and (iii). this approach need to be compatible with in house vector system, a structure of AgeI site–NsiI site-Inserted gene–BspEI site–TAATAG–NotI site was formed. A module with particular nucleic acid sequence in both ends of each domain is shown in Figure 2. When a single domain is inserted into a vector, NotI and NsiI were used(the domain remains from shadow area of B to shadow area of E). When more than one domains were planned to be inserted, the first one should be digested by NsiI and BspEI (from B to C) and the last one should be digested by AgeI and NotI (from A to E). The restriction enzymes AgeI and BspEI were used in pair when fusing domains together. A scar area of (a combination of unshadow area of A and C) was formed, which cannot be digested by AgeI or BspEI anymore. During expression, the nucleotides of the connection part (scar+ site B) would be translated into amino acid sequence of Ser-Gly-Met-His, whose structure we expected to be relatively simple thus won’t change the structure of original domain severely as an additional part. Therefore, this assembly strategy ensures that there oare no frameshifts between the domians.

Figure 2: Module of gBlocks. Shadow area of sequence A was restriction site for AgeI while B for NsiI, C for BspEI and E for NotI. Sequence D consists of two stop codons which ensure the inserted domain be expressed precisely.

Research Methods

gBlocks and codon optimized

The nucleic acid chains for most domains are too big to be cloned using gBlocks, which are double-stranded, sequence-verified genomic blocks up to 750bp in length. The sizes are 448, 492, 321, 375, 815, 91 and 496 AA for KS, MAT, DH, MT, KR, ACP, CON domains respectively. Thus each domain should still be split into parts, making corresponding DNA fragments in a form of 500bp or 750bp which were produced by IDT (Integrated DNA Technologies). The design of those fragments also included restriction site attached to both ends of the domain and an overlap of 42bp for fragments belong to one domain.

DNA assembly

Gibson assembly allows for successful assembly of multiple DNA fragments, so we use it to fuse two or three DNA fragments together for a complete domain. A combination of 25 ng of backbone vector (pJet1.2 blunt end) with 50 ng of insert fragments (G-blocks) and adequate amount of MiliQ water (depends on the number of gBlocks inserted) to make 10µL in total, was incubated with 10µL 2X Gibson Assembly Master Mix in a final volume of 20µL. The samples were incubated at 50 °C temperature for one hour before transformed into competent cells.

Colony PCR

After ligation, competent cells were transformed and subsequently transferred to LB agar plates containing ampicillin as a selection marker in a concentration of 0.1%. Successful transformants were identified using colony pcr. 8 single colonies for each assembled domain were chosen for further PCR analysis. 1% agarose gel was used to separate fragments of different size apart.

Preparation of plasmid

The reagents and protocol from a Miniprep Kit of Thermo was used to isolate plasmid. After, the plasmid concentration was measured by Nano drop.

Digestion

Restriction enzymes from NEB (New England Biolabs) were used for digesting fragments. The digested fragments would be inserted into a vector for gene expression in fungi. According to the designed structure of gBlocks which was mentioned earlier, NotI and NsiI were used for inserting single domain into vector, while AgeI and BspEI were used to form scar area while more than one domain would be fused together. The protocol was obtained from double digestion manual of NEB.

Purification of DNA fragment

After digestion, a 1% agarose gel was used for DNA extraction. After the DNA fragments with different sizes were separated on the gel, the band with the expected size was cut out. The reagents and protocol from Gel extraction Kit of Thermo were used to purify the fragment, then the concentration of fragment was measured by Nano drop.

Results

Colony PCR confirmed the succesful assembly of Gblocks of each domain, shown in Figure 3. Correct assembly fragments could be obtained.

Figure 3: Colony PCR results for the domains.

The ligation of KS domain in vector is confirm by observing the band in the expected size, shown in Figure 5.

Figure 4: Successful ligation of KS domain.

To confirm the expected potential to be a lovastatin producer, the lovastatin resistance of A. niger was tested. The fungus was incubated on plates with different concentrations of lovastatin.

Figure 5: Lovastatin plate with A. niger on it.

Future perspective

The production medium of lovastatin in Aspergillus niger was designed with xylose as the carbon source. After LovB gene is inserted into A. niger, the expression level could be detected. Additionally, the combination of LovB, LovC, LovG and even other necessary lov enzymes together is feasible and result in a super lovastatin productive enzyme.

References

1.Tobert, J. A. (2003). Lovastatin and beyond: The history of the HMG-CoA reductase inhibitors. Nature Reviews Drug Discovery, 2(7), 517-526.
2.Campbell, C. D., & Vederas, J. C. (2010). Biosynthesis of Lovastatin and Related Metabolites Formed by Fungal Iterative PKS Enzymes. Biopolymers, 93(9), 755-763.
3.Xu, W., Chooi, Y. H., Choi, J. W., Li, S., Vederas, J. C., Da Silva, N. A., & Tang, Y. (2013). LovG: The Thioesterase Required for DihydromonacolinL Release and Lovastatin Nonaketide Synthase Turnover in Lovastatin Biosynthesis. Angewandte Chemie-International Edition, 52(25), 6472-6475.
4.Ames, B. D., Nguyen, C., Bruegger, J., Smith, P., Xu, W., Ma, S., Tsai, S. C. (2012). Crystal structure and biochemical studies of the trans-acting polyketide enoyl reductase LovC from lovastatin biosynthesis. Proceedings of the National Academy of Sciences of the United States of America, 109(28), 11144-11149.
5.Ma, S. M., & Tang, Y. (2007). Biochemical characterization of the minimal polyketide synthase domains in the lovastatin nonaketide synthase LovB. Febs Journal, 274(11), 2854-2864.